Electron-Nuclear Double Resonance Study of the Zinc Vacancy in Zinc GERMANIUM PHOSPHIDE (ZnGeP2)

1997 ◽  
Vol 484 ◽  
Author(s):  
K. T. Stevens ◽  
S. D. Setzler ◽  
L. E. Halliburton ◽  
N. C. Fernelius ◽  
P. G. Schunemann ◽  
...  
Keyword(s):  
Hyperfine Interactions ◽  
Double Resonance ◽  
Zinc Vacancy ◽  
Electron Nuclear Double Resonance ◽  
Paramagnetic Resonance ◽  
Principal Axes ◽  
Zinc Germanium Phosphide ◽  
Epr Signal ◽  
Electron Paramagnetic ◽  
Additional Hyperfine

AbstractAs-grown crystals of ZnGeP2 are highly compensated and contain significant concentrations of donors and acceptors. The dominant acceptor in ZnGeP2 is believed to be the zinc vacancy. This center is paramagnetic in its normal singly ionized state, and gives rise to an electron paramagnetic resonance (EPR) signal characterized by a resolved primary hyperfine interaction with two equivalent phosphorus nuclei adjacent to the vacancy. The present investigation has focused on electron-nuclear double resonance (ENDOR) measurements of additional hyperfine interactions which are not resolved in the regular EPR spectra. Principal values and principal axes directions for four additional phosphorus nuclei are determined from the ENDOR angular dependence. These parameters support the zinc-vacancy assignment for the acceptor and they provide an experimental check of wave functions generated in future computational modeling efforts.

The Microscopic Structure Of Shallow Donors In Silicon Carbide

1996 ◽  
Vol 442 ◽  
Author(s):  
J.-M. Spaeth ◽  
S. Greulich-Weber ◽  
M. März ◽  
E. N. Kalabukhova ◽  
S. N. Lukin
Keyword(s):  
High Temperature ◽  
Low Temperature ◽  
Temperature Dependence ◽  
Double Resonance ◽  
Epr Spectra ◽  
Electron Nuclear Double Resonance ◽  
Paramagnetic Resonance ◽  
Vacancy Pair ◽  
Temperature Spectra ◽  
Electron Paramagnetic

AbstractThe electronic structure of nitrogen donors in 6H-, 4H- and 3C-SiC is investigated by measuring the nitrogen hyperfine (hf) interactions with electron nuclear double resonance (ENDOR) and the temperature dependence of the hf split electron paramagnetic resonance (EPR) spectra. Superhyperfine (shf) interactions with many shells of 13C and 29Si were measured in 6H-SiC. The hf and shf interactions are discussed in the framework of effective mass theory. The temperature dependence is explained with the thermal occupation of the lowest valley-orbit split A1 and E states. It is proposed that the EPR spectra of P donors observed previously in neutron transmuted 6H-SiC at low temperature (<10K) and high temperature (>60K) are all due to substitutional P donors on the two quasi-cubic and hexagonal Si sites, whereby at low temperature the E state is occupied and at high temperature the A1 state. The low temperature spectra are thus thought not to be due to P-vacancy pair defects as proposed previously.

scholarly journals The binuclear cluster of [FeFe] hydrogenase is formed with sulfur donated by cysteine of an [Fe(Cys)(CO)2(CN)] organometallic precursor

2019 ◽  
Vol 116 (42) ◽  
pp. 20850-20855 ◽  
Author(s):  
Guodong Rao ◽  
Scott A. Pattenaude ◽  
Katherine Alwan ◽  
Ninian J. Blackburn ◽  
R. David Britt ◽  
...  
Keyword(s):  
Double Resonance ◽  
Electron Nuclear Double Resonance ◽  
Paramagnetic Resonance ◽  
Carbon And Nitrogen ◽  
Binuclear Cluster ◽  
Organometallic Precursor ◽  
Pulse Epr ◽  
X Ray Absorption ◽  
Electron Paramagnetic

The enzyme [FeFe]-hydrogenase (HydA1) contains a unique 6-iron cofactor, the H-cluster, that has unusual ligands to an Fe–Fe binuclear subcluster: CN−, CO, and an azadithiolate (adt) ligand that provides 2 S bridges between the 2 Fe atoms. In cells, the H-cluster is assembled by a collection of 3 maturases: HydE and HydF, whose roles aren’t fully understood, and HydG, which has been shown to construct a [Fe(Cys)(CO)2(CN)] organometallic precursor to the binuclear cluster. Here, we report the in vitro assembly of the H-cluster in the absence of HydG, which is functionally replaced by adding a synthetic [Fe(Cys)(CO)2(CN)] carrier in the maturation reaction. The synthetic carrier and the HydG-generated analog exhibit similar infrared spectra. The carrier allows HydG-free maturation to HydA1, whose activity matches that of the native enzyme. Maturation with 13CN-containing carrier affords 13CN-labeled enzyme as verified by electron paramagnetic resonance (EPR)/electron nuclear double-resonance spectra. This synthetic surrogate approach complements existing biochemical strategies and greatly facilitates the understanding of pathways involved in the assembly of the H-cluster. As an immediate demonstration, we clarify that Cys is not the source of the carbon and nitrogen atoms in the adt ligand using pulse EPR to target the magnetic couplings introduced via a 13C3,15N-Cys–labeled synthetic carrier. Parallel mass-spectrometry experiments show that the Cys backbone is converted to pyruvate, consistent with a cysteine role in donating S in forming the adt bridge. This mechanistic scenario is confirmed via maturation with a seleno-Cys carrier to form HydA1–Se, where the incorporation of Se was characterized by extended X-ray absorption fine structure spectroscopy.

Electron paramagnetic resonance and electron-nuclear double resonance study of Mn2+ ions in CdGeAs2 crystals

2006 ◽  
Vol 243 (15) ◽  
pp. 4070-4079 ◽  
Author(s):  
S. M. Evans ◽  
N. Y. Garces ◽  
R. C. DeMattei ◽  
R. S. Feigelson ◽  
K. T. Zawilski ◽  
...  
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Double Resonance ◽  
Electron Nuclear Double Resonance ◽  
Paramagnetic Resonance ◽  
Electron Paramagnetic
Sign in / Sign up

Export Citation Format

Share Document